Recent advances in quaternary copper-based sulfides and their derivatives for solar hydrogen evolution

Abstract

Quaternary copper-based sulfides (QCSs) exhibit significant potential for solar hydrogen evolution due to their diverse compositions and structures, suitable band structure, controllable synthesis, and non-toxic nature. Strengthening cognition for nanostructures enables the fabrication of high-efficiency photocatalysts. Although a comprehensive understanding of photocatalytic processes of QCSs-based photocatalysts has been recently accumulated, the correlation between structure and function remains incompletely elucidated. This overview begins with an introduction to the fundamental principles of solar hydrogen evolution. Subsequently, we provide a succinct description of the controllable synthesis of QCSs-based photocatalysts. The structure-function correlation of single QCSs is systematically discussed by exploring how structure-related properties influence photocatalytic processes. Recent advancements based on the single QCSs are summarized in detail. As the guide, we further discussed the structure-function correlation of QCS-based derivatives including semiconductor heterojunctions, cocatalyst loading, heteroatomic doping, and polytypic homojunctions. Different mechanisms of activity enhancement are provided along with a summary of their research progress in solar hydrogen evolution. In conclusion, challenges and perspectives for material synthesis and energy conversion are proposed. We anticipate that this overview will offer valuable insights for future exploration of QCS-based photocatalysts, greatly advancing the progress in this emerging research field.

Article information

Article type
Review Article
Submitted
06 Чер 2024
Accepted
19 Лип 2024
First published
19 Лип 2024

J. Mater. Chem. A, 2024, Accepted Manuscript

Recent advances in quaternary copper-based sulfides and their derivatives for solar hydrogen evolution

Y. Li, Z. Liu, J. Chen, S. Wang, O. Lin, C. Yang, Z. Yin and A. Tang, J. Mater. Chem. A, 2024, Accepted Manuscript , DOI: 10.1039/D4TA03912B

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